Medlon, Inc.
PROCESS CHANGE
SKU K810721UPC FPA
In Stock
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IIFDA 510(k) Cleared (K810721)
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Free shipping on orders over $99 · 30-day returns
Medlon, Inc.
Free shipping on orders over $99 · 30-day returns
PROCESS CHANGE is an FDA 510(k)-cleared medical device (K810721) manufactured by Medlon, Inc.. This device is classified under the General Hospital specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 22, 1981. Regulation: 8.
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